NDC 10702-108

Dexmethylphenidate Hydrochloride 10 mg tablet

On the label: KVK-TECH, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Kvk-Tech, Inc.Newtown, PA, United StatesMakes it Serious problems, FDA actionMar 14, 2025 · 13 inspections, 3 with FDA action

Product details

Generic drug
Dexmethylphenidate: every company that makes it
Form
tablet, oral
Strength
10 mg
Approval
ANDA ANDA206931
On the market since
Dec 4, 2015
Package NDCs
10702-108-01
Official label
DailyMed (National Library of Medicine), updated Nov 24, 2025

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